ES2357084T3 - SYSTEMS AND METHOD TO THERMALLY PROFILE RADIO FREQUENCY ELECTRODES. - Google Patents

Abstract

A system for the thermal or electromagnetic treatment of an objective surgical site (D), the system comprising: a cannula (102) having a proximal and a distal end; a probe (104) for the release of energy having a proximal and a distal end, the probe being able to be selectively advanced within the cannula to expose the distal end of the probe from the distal end of the cannula; and characterized in that: a set of images (200) that includes a plurality of layers (202n), each layer including an image representing a treatment profile for the probe, the treatment profile estimating a therapeutic treatment depth by the activation of the probe, in which the image of each layer represents a thermal profile (150) surrounding the exposed distal end of the probe.

Description

BACKGROUND

1. Technical field

The present disclosure relates to systems and methods for providing radiofrequency energy ("RF") to biological tissue and, more particularly to systems and methods for thermally profiling radiofrequency electrodes 5 used in surgical procedures using RF.

2. Background of the prior art

The use of radiofrequency energy ("RF energy") and, in particular, radiofrequency electrodes ("RF electrodes") for the removal of tissue in the body or for the treatment of pain is known. Generally, such RF electrodes (for example probes, resistance heating elements and the like) 10 include a configuration for insertion into the body in the tissue to be treated or removed. RF electrodes may also include an exposed conductive tip part and an insulated part. Therefore, when the RF electrode is connected to an external source of radiofrequency power (for example an electrosurgical generator), the heating of the tissue occurs near and around the exposed conductive tip portion thereof, so that they are created therapeutic changes in the target tissue, near the conductive tip due to the rise in tissue temperature.

The use of thermal therapy in and around the spine is also known. It is convenient to treat the posterior or postero-lateral part of the intervertebral disc for the indication of mechanical degeneration of the disc and discogenic back pain. The pain may be due to degeneration or compression of the intervertebral disc in its posterior or postero-lateral parts. There is some innervation of the intervertebral disc near the surface of the disc and also within its outer part known as the fibrous ring. Mechanical damage such as fissures or cracks inside the disc caused by age or mechanical trauma can lead to innervation of the disc, which is believed to be associated with painful symptoms.

Heating in an intervertebral disc to relieve such painful symptoms is described in US Patent No. 5,433,739 and in US Patent No. 5,571,147, both of Sluijter et al. In these patents, electrodes 25 are described in radiofrequency heating or in resistance heating of all or part of the intervertebral disc. Flexible, straight or curved tip electrodes are described for this purpose.

An intervertebral disc apparatus for the treatment of an intervertebral disc has been disclosed in US Patent No. 6,007,570. The apparatus includes a catheter having an intradiscal section in the form of a helical spring. In use, the intradiscal section is advanced through the nucleus pulposus and is manipulated to navigate within the nucleus along the inner wall of the fibrous ring. An element that releases energy incorporated into the apparatus adjacent to the intradiscal section supplies energy to treat the disc area.

WO 01174252 discloses an apparatus for treating a tumor, which includes an elongated release device. A sensing device can be deployed from the elongated release device to distinguish the type of tissue and to determine an amount of tumor removal. 35

There is a continuing need for improved electrosurgical and particularly RF energy procedures that use the thermal profile of the radiofrequency electrodes for the placement of the radiofrequency electrode and the display of the area and / or treatment area of the radiofrequency electrode. There is also a continuing need for improved thermal profile systems of radiofrequency electrodes used in surgical procedures that use RF energy. 40

SUMMARY

The present invention is directed to new and improved systems for thermally profiling radiofrequency electrodes.

A system for the thermal or electromagnetic treatment of an objective surgical site, in accordance with a preferred embodiment of the present disclosure, includes a cannula having a proximal end and a distal end, a probe 45 for releasing energy having a proximal end and a distal one, the probe being able to selectively advance into the cannula to expose the distal end of the probe from the distal end of the cannula, and an image file that includes a plurality of layers, each layer including an image representing a profile of treatment for the probe, estimating the treatment profile a depth of therapeutic treatment by the activation of the probe. fifty

The image of each layer represents a thermal profile. The thermal profile preferably surrounds the exposed distal end of the probe. The layer is preferably a digital representation. The distal end of the probe can be exposed from the distal end of the cannula and the digital representation is conveniently scaled.

The system according to the present embodiment may further include an imaging system to form the image of the target surgical site. The imaging system may include a monitor to visualize the image of the target surgical site. The imaging system is an operational association with the set of layer images. Preferably, each layer can be superimposed on the image of the target surgical site. 5

The probe is adapted to be connected to a power source. The power source can be adjusted to vary at least one operational setting. Operational settings may include at least one of temperature, impedance, RF power, RF current intensity, RF voltage, operating mode and application duration.

The system according to the present embodiment may further include a layer for each amount of exposure of the distal end of the probe from the distal end of the cannula. At least one layer for each amount of exposure 10 of the distal end of the probe may include at least one layer for each operational setting of the power source.

A method of creating a layer for performing surgical procedures is exposed. Such a method does not constitute an embodiment of the present invention. The method includes the steps of providing a heat collection system. The heat collection system includes a bath that contains an amount of a test gel, at least one sheet of thermally reactive paper, a probe that can be connected to a power source and capable of releasing energy, and a obtaining system of images / data operatively attachable to the power source and directed towards the bathroom.

The method also includes the steps of stabilizing the bath temperature, placing a piece of thermal reactive paper inside the bath, placing the probe inside the bath so that the test is arranged between the thermal reactive paper 20 and the imaging system / data, activate the power source, and record the image created on the thermal reactive paper and the parameters associated with the power source with the image / data collection system.

Registered parameters include, and are not limited to, at least the temperature, impedance, RF power, RF current intensity, RF voltage, mode of operation, amount of exposure of the probe from a distal end of the cannula, and duration of activation of the power source. The method also includes the storage step of the layer that includes the image and the parameters in a set of images.

Preferably, the layer is stored digitally. The method also includes the step of creating a plurality of layers by repeating the method for each parameter and registering the image and the associated parameters.

The thermally reactive paper is a thermal liquid crystal paper. The thermal liquid crystal paper is sensitive in the range of 25 ° C-100 ° C, more particularly, approximately in the range 35 ° C-100 ° C.

According to the method, the cannula may have a typical exposure tip of the cannula being used. For example, about 2-50 mm, more preferably about 3-6 mm.

A method of treating an objective surgical site is exposed. Such a method does not constitute an embodiment of the present invention. The method includes the steps of providing at least one layer that includes an image that represents a treatment profile of a probe, the treatment profile providing an estimate of a depth of a therapeutic treatment by the activation of a probe corresponding to the probe. probe of the respective layer, and superimposing at least one layer on an image scan of the surgical treatment site in order to visualize the depth of the therapeutic treatment that can be applied with a probe configured according to the treatment profile of at least one respective layer. 40

The method further includes the step of providing a plurality of layers, each layer representing a treatment profile corresponding to one of a plurality of probe configurations and unique intensity settings. The method includes the step of providing a probe capable of releasing energy. The probe can be selectively advanced into a cannula to expose a distal end of the probe from a distal end of the cannula. The method also includes the step of providing an electrosurgical energy source. The probe can be selectively connected to the electrosurgical energy source.

The method further includes the steps of forming the image of the target surgical site, and of superimposing at least one of the layers on the image of the target surgical site. The method includes selecting a layer that represents a treatment profile that corresponds to the therapeutic treatment and the desired resulting effect.

The method further includes the steps of introducing the probe into the target surgical site according to the treatment profile 50 of the selected layer, and activating the probe according to the treatment profile of the selected layer.

These and other aspects and advantages of the exhibition will be more evident from the following detailed description and the accompanying drawings, which illustrate by way of example the characteristics of the foregoing.

BRIEF DESCRIPTION OF THE DRAWINGS

The characteristics of the system and the method of the present exhibition will become more readily apparent and may be better understood by reference to the following detailed descriptions of illustrative embodiments of the present exhibition, taken in conjunction with the accompanying drawings, in which:

Figure 1 is a straight sectional view of an intervertebral disc with a portion of the intervertebral apparatus of the present exposure inserted in the intervertebral disc;

Figures 2a, 2b, and 2c show a system of components of the intervertebral apparatus of Figure 1 for RF heating of the intervertebral disc or any other RF heating, thermal removal, or cryogenic denervation, including the apparatus a cannula, an impedance stylet , and an electrode;

Figure 3 is a flow chart illustrating a method of creating a database of thermal profile layers 10;

Figure 4 is a schematic view of a heat collection system for creating a thermal profile layer in accordance with the present disclosure;

Figure 5 is an enlarged schematic illustration depicting the creation of an image of a thermal profile; fifteen

Figure 6 is an example of a thermal profile image produced by the thermal collection system of Figure 4;

Figure 7 is a schematic illustration of a system for performing surgical procedures using the thermal profile;

Figure 8 is a flow chart illustrating examples of methods of surgical procedures of embodiment using thermally profiled electrodes;

Figure 9 is a schematic illustration of a step of the method of Figure 8;

Figure 10 is a schematic illustration of another step of the method of Figure 8;

Figure 11 is a schematic illustration of another step of the method of Figure 8;

Figure 12 is an enlarged schematic illustration of the indicated area of Figure 11; 25

Figure 13 is a fluoroscopic image of a spine illustrating a spinal needle that is being inserted from the left into the pulposus nucleus of a vertebral disc, and of an introducer cannula and an electrode being inserted from the right into the fibrous ring of the vertebral disc;

Figure 14 is a fluoroscopic image of the spine of Figure 13 illustrating a layer, in accordance with the present exposure, superimposed on the electrode to provide a visualization of the predicted zone 30 of the thermal effect;

Figure 15 is an enlarged fluoroscopic image illustrating the electrode / thermal profile of the layer of Figure 14; Y

Figure 16 is a layer illustrating the histology of the tissue along with the actual thermal effects produced by the treatment. 35

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

The systems and methods of the present exposure facilitate a more precise controlled placement of a thermal probe in an intervertebral disc set as a treatment target. In addition, the systems and methods of the present disclosure facilitate an improved ability to predict and / or visualize the depth of treatment possible by the thermal probe when set for the various operating parameters. 40

It will be readily apparent to a person skilled in the art that systems and methods of using the systems can be used to treat / destroy body tissues in any body cavity or tissue sites that are accessible by percutaneous or endoscopic catheters or open surgical techniques, and are not limited to the area of the disc and / or the spine. It is intended that the applications of the systems and methods in all these organs and tissues be included within the scope of this exhibition. Four. Five

Before a detailed discussion of the system and methods of use of the systems and method of the present exhibition, a brief overview of the anatomy of the intervertebral disc is shown. With reference to Figure 1 an intervertebral disc "D" has a fibrous ring "A" and a pulpy core "N" disposed within the fibrous ring "A". Fibrous ring "A" includes a hard fibrous material that is arranged to define a plurality of cartilaginous rings "R"

that form the natural striated tissue of the ring. The nucleus pulposus "N" consists mainly of an amorphous gel that has a softer consistency than that of the fibrous ring "A". The nucleus pulposus "N" usually contains 70% -90% by weight of water and works mechanically like an incompressible hydrostatic material. The junction or transition zone of the fibrous ring "A" and the nucleus pulposus "N" generally defines, for discussion purposes, an internal wall "W" of the fibrous ring "A". The crust of the disc "C" surrounds the fibrous ring "A". The posterior, anterior and lateral parts of the intervertebral disc "D" are identified as "P", "AN" and "L", respectively, with the opposite postero-lateral orientations identified as "PL".

When mechanical tension is applied to an intervertebral disc or when an intervertebral disc degenerates with age, fissures (illustrated by cracks "F" in Figure 1) may occur on the posterior or postero-lateral parts of the disc "D". Problems with nerves, "F" fissures and degenerative discs can lead to various problems in 10 patients, such as back or leg pains caused by irritation or occurrence of these abnormalities. In addition, these conditions may ultimately lead to states such as bulging or disc herniations. Heat and / or electromagnetic field (EMF) therapy of the intervertebral disc "D", preferably, the fibrous ring "A" in the posterior "P" or postero-lateral "PL", will lead to nerve denervation and / or alterations and the thermal removal of disc structures, which in turn will produce pain relief and disc heating. Thus, it is desirable to insert and place a thermal or electromagnetic probe on the back "P" and / or postero-lateral "PL" of the intervertebral disc "D" when these neural and abnormal structures occur for pain relief and other problems related to the disk.

1. Thermal profiling system in the surgical electrode

In the drawings and in the description that follows the term "next", as is traditional, it will refer to the end of the system, or component of it, which is closer to the operator, and the term "distal" will refer to the end of the system, or component of it, that is farther from the operator.

With reference to Figure 1, according to an embodiment of the present disclosure, an RF energy use system and thermal profile in surgical procedures are generally designated as 100. The system 100 includes an outer insert or introducer cannula 102, a probe for the release of energy (for example, electrode, thermal probe, EMF probe, electrosurgical probe, etc.) 104 which can be placed inside the cannula 102, an electrosurgical generator , a power source or the like 106 connected to the probe 104. Optionally, the system 100 may include an impedance stylet 108 which can also be placed inside the cannula 102.

As seen in Figures 1 and 2a, the introducer cannula 102 preferably includes a rigid tubular shaft 110 defining a longitudinal axis "X". The tubular shaft 110 preferably includes a beveled tip 112 contiguous with its distal end 114 and oblique with respect to the longitudinal axis "X". Preferably, the beveled tip 112 is oblique from about 15 ° to about 45 °. The shaft 110 is preferably composed of a conductive material such as stainless steel or other suitable compound and is insulated with insulation 116 along at least one part, preferably, along most of its length. Alternatively, shaft 110 may be made from an appropriate polymeric material and formed by conventional injection molding techniques. 35 The distal end 114 of the shaft 110 may be left uninsulated or exposed to allow electrical communication with the tissue when the cannula 102 is placed in the tissue, (for example, for impedance measurement, etc.). A handle or recess 118 is preferably connected to a proximal end of the cannula 102 and may include a reference marker 120 to indicate the direction of the beveled tip 112, so that when the probe 104 is inserted into the cannula 102 the surgeon it can determine in which azimuthal rotational direction the beveled tip 112 40 is oriented.

The axis 110 may have a diameter from a fraction of a millimeter to several millimeters and a length of a few centimeters to about 20 centimeters or more. Alternatively, shaft 110 may be made of a MRI (Magnetic Resonance Imaging) compatible material, which includes cobalt, titanium, copper, Nitinol, etc. alloys. Four. Five

The power source or generator 106 may be, for example, a radio frequency generator that provides power at a frequency between several kilohertz to several hundred megahertz. The generator 106 can have a power output from several watts to several hundred watts, depending on the clinical needs. The generator 106 may have control devices for increasing or modulating the power output as well as reading and display devices for monitoring energy parameters such as voltage, current intensity, power, frequency, temperature, impedance, etc, valued by one skilled in the art. Other types of power sources and / or generators are considered, for example, which include and are not limited to resistance heating units, laser sources, or microwave generators.

The probe (eg thermal probe or EMF) 104 of system 100 will be discussed with continued reference to Figures 1 and 2a-2c. As seen in Figures 1 and 2c, electrode 104 can be placed inside cannula 102 and It can be adapted for reciprocal movement between them. When a radiofrequency probe is used, probe 104 is a monopolar system and is used in conjunction with an extended surface area grounding pad 134 (see Figure 13) that makes contact with the patient's skin over a very superficial surface area. wide relative to the exposed surface of the electrode tip. In addition, when used as a radiofrequency probe, the electrode

104 can be isolated except in a distal part of it that can be left uninsulated for energy transmission. Alternatively, and in a preferred embodiment, the probe 104 may be totally uninsulated, while the cannula 102 functions as the insulating element of the apparatus. In this arrangement the degree of extension of the distal end portion of the probe 104 beyond the beveled tip 112 determines the heating capacity of the electrode 104. The probe 104 includes a handle 130 and an elongate element or rod 132 that extends distally 5 from the handle 130. An exemplary embodiment of a thermal probe or EMF is provided by US Patent No. 6,604,003 to Fredricks et al.

As seen in Figures 1 and 2b, the impedance stylet 108 can be placed in the cannula light 102 and preferably closes the front opening of the cannula 102 to prevent the entry of tissue, fluids, etc., during the introduction of the cannula 102 inside the intervertebral disc "D". The stiletto 108 may include a head 140 that coincides with the housing 118 of the cannula 102 into which the stylet 108 is inserted to monitor the impedance of the tissue adjacent to the distal end of the cannula 102. Once the combination of the stiletto 108 and of the cannula 102 has been inserted into the body the impedance monitoring helps to determine the position of the beveled tip 112 of the cannula 102 with respect to the patient's skin, the cortex "C", the fibrous ring " A ”, and / or the nucleus“ N ”of the intervertebral disc“ D ”. Each of these zones will have different impedance levels, which are quickly quantifiable.

For example, for a fully insulated electrode or cannula with an exposed area of a few millimeters at the end of the cannula, the impedance will change significantly from the position of the tip near or that makes contact with the cortex "C" of the intervertebral disc "D" to the area where the tip is inside the fibrous ring "A" and also where the tip is inside the nucleus "N" of the intervertebral disc "D". The impedance differences may range from a few hundred ohms outside the intervertebral disc "D" from 200 to 300 ohms in the fibrous ring "A" to about 100 to 200 ohms in the "N" core.

This variation can be detected by the surgeon visualizing the impedance in meters or hearing an audio tone whose frequency is proportional to the impedance. Such tone can be generated by a monitor (not shown). In this way, an independent means for detecting the placement of the cannula 102 within the intervertebral disc 25 "D" is provided. Thus, for example in an application in which an electrode 104 in the form of an EMF probe is to be inserted between adjacent layers of annular tissue, the unwanted penetration of the tip of the EMF probe 104, which extends from the cannula 102 through the inner wall "W" of the ring "A" and into the pulpy core "N", can be detected by means of impedance monitoring.

As seen in Figures 1, 4 and 7, the system 100 further includes a set of images 200 having a plurality of profiles / layers 202. As used herein, the term "set of images" is understood as including, and It is not limited to, a file repository, database, database, hidden memory, storage unit or similar. Each layer 202 includes a thermal profile that is characteristic of, and / or specific to, a particular configuration of a channel / electrode assembly or amount of exposure (i.e., specific to the amount of probe 104 extending from the distal tip of cannula 102) of the channel / electrode assembly. In addition, for each quantity of exposure or configuration of the channel / electrode assembly, a plurality of layers 202n is provided that includes a thermal profile that is related to, for example, the amount of time that the probe 104 is activated, with the temperature to which probe 104 is heated, etc.

As seen in Figure 7, the system 100 further includes an imaging system 300 configured and adapted to form an image of and visualize the target surgical site. The 40 imaging system 300 includes an imaging device 302 in the form of an X-ray imager, a CT scanner, an MRI device, a fluoroscopic imager and the like, and a monitor 304 to visualize the image produced by the imaging device 302. Preferably, the image set 200 is connected to the imaging system 300.

2. Method of creating a thermal layer 45

Turning now to Figures 3-6, a method of creating a thermal layer 202, of the plurality of thermal layers 202n, is illustrated and described. The creation of a thermal layer 202 includes the step of providing a collection system 400, preferably a thermal collection system. The thermal collection system 400 includes a bath 402 containing an amount of a transparent test gel 404 (for example, a conductive polymer of formula SMK / RFK), a gadget 406 configured and adapted to support a cannula / probe assembly 102 / 104 and a piece of 50 thermal reactive paper, preferably a thermal liquid crystal (LC) paper 408, an electrosurgical generator 410 operatively connected to the cannula / electrode assembly 102/104, and an image / data collection system 412 operatively connected to electrosurgical generator 410 and oriented towards bath 402.

The method of creating a thermal layer 202 also includes the steps of:

 stabilize the temperature of test gel 404 in bath 402 at approximately 30 ° C; 55

 coupling the cannula / probe assembly 102/104 and the LC 408 paper to the gadget 406, so that the cannula / probe assembly 102/104 and the LC 408 paper are positioned next to each other, preferably at a predetermined distance;

 place (for example, submerging) the cannula / probe assembly 102/104 and the LC 408 paper in the bath 402 so that the cannula / probe assembly 102/104 is arranged between the LC 408 paper and the imaging system / data 412;

 set electrosurgical generator 410 in a "lesion" or continuous mode graduation at a temperature of about 42 ° C or about 80 ° C; 5

 activate and / or stimulate the electrosurgical generator 410, so that the thermal radiation emanating from the probe 102 hits the LC paper 408 to create a thermal image "TI"; Y

 record, with the image / data collection system 412, the image (ie temperature gradients or "halos" 150 around the cannula / probe assembly 102/104) created on the LC 408 paper and record the parameters of input (for example, temperature, impedance, RF power, intensity of the RF current, RF voltage, mode of operation, exposure of the probe 104 from the distal end of the cannula 102, duration of the application of electrosurgical energy, etc. ) associated with the creation of the image on the LC 408 paper.

As can be seen in Figure 5, the temperature gradients or "halos" 150 formed on the LC 408 paper include a plurality of "halos" 150 of different color, each color representing a different temperature. The temperature at which the electrosurgical generator 410 is set will determine the LC paper that is used, for example for a temperature graduation of 42 ° C the LC paper having a range of 35 ° -40 ° C is used, and for a temperature graduation of 80 ° C LC paper having a range of 55 ° -60 ° C is used. Preferably, a thermal imaging camera or the like is used to record the temperature gradients produced on the LC 408 paper.

Preferably, the thermal image "TI" and the data provided by the thermal image "TI" are recorded digitally. Therefore, the method of creating a layer 202 may also include the step of storing, preferably in digital format, the image and the data in the set of images 200.

The process is repeated to create a layer 202 for each cannula / probe assembly 102/104 configuration and each graduation. In this way, a plurality of layers 202n is created and stored in memory 200. For example, a series of layers 200 can be created for each temperature setting of electrosurgical generator 410 (for example 42 ° C and 80 ° C). For each temperature graduation of the electrosurgical generator 410, a series of layers 200 can be created for each exposure dimension of the tip (for example, 3, 4 and 6 mm) of the cannula 102. For each exposure dimension of the cannula 102 a series of layers 200 can be created for each displaced position of the probe 104 relative to the cannula 102. The displacement positions are referenced with the "level" state 30 (ie 0 mm) that is obtained by placing a surface flat with the chamfer of the cannula 102 and inserting the probe 104 into the cannula 102 until the probe makes contact with the flat surface.

As seen in Figure 6, the shapes of the "TI" thermal images are usually elliptical and centered on the exposed tip of the probe 104. The major axis of the ellipse can be measured using a software analysis software images. The thermal image "TI" is represented by a series of gradations or rings 150, 35 each ring 150 representing a different temperature intensity.

The creation of the thermal layers according to the present method provides visual information that will help to compare the operation between the different electrodes and the different electrosurgical generators.

While the method described above is a preferred method of creating a thermal layer, it has been considered that other methods are also possible. For example, it has been considered that a thermally sensitive gel or paint (for example, a compound containing in it amounts of a thermally sensitive substance) can be applied to the surface of a tissue sample (for example, a tissue of a human corpse , a pig tissue or similar). The cannula / probe assembly 102/104 can then be introduced into the tissue of the sample and the electrosurgical generator 410 can be activated according to the method described above in order to create a thermal profile on the surface of the tissue sample. The thermal profile can be registered in a manner similar to that of the method described above. This procedure can be repeated as many times as necessary in order to produce thermal profiles for different depths of insertion of the cannula / probe 102/104 into the sample tissue, for various graduations of the electrosurgical generator 410, and / or for the various configurations of the cannula / probe assembly 102/104. In this way, the effects of the cannula / probe assembly 102/104 can easily be represented in the tissue.

3. Method of performing surgical procedures

Before a detailed discussion of the methods of performing surgical procedures in accordance with the present discussion, a brief overview of a general method of performing a heat treatment of an intervertebral disc is presented. With reference to Figure 1, the target intervertebral disc "D" 55 is identified during a preoperative phase of a surgical operation. Next, access to the intervertebral disc area is verified, preferably by percutaneous techniques or, less preferably, by techniques

Open surgical The cannula 102, with the stylus 108 positioned and fixed therein, is inserted into the intervertebral disc "D", preferably from a posterior or postero-lateral place. Alternatively, cannula 102 can be used without stylet 108.

During the introduction of the cannula / stylet assembly 102/108, the impedance of the tissue adjacent to the distal end of the cannula 102 is monitored. The impedance monitoring of the adjacent tissue can be used to determine the position of the tip of the cannula 102 with with respect to the patient's skin, the cortex "C", the fibrous ring "A" and / or the pulpy nucleus "N" of the intervertebral disc "D". As stated above, these zones have different and quantifiable impedance levels, so they provide an indication to the user of the position of the tip of the cannula 102 in the tissue. The monitoring of the position of the tip of the cannula 102 can also be confirmed with the use of the imaging system 300. Typically, the tip of the cannula 102 is located 10 within the fibrous ring "A" of the intervertebral disc "D "In a postero-lateral position" PL "of the intervertebral disc" D "without penetrating through the internal wall" W "or in the core" N ".

With the cannula 102 in the desired position, the stylet 108 is removed and the probe 104 is placed inside the cannula 102 and advanced therethrough. The probe 104 is advanced enough to expose at least partially a distal portion thereof from the tip of the cannula 102. The degree of exposure of the distal end portion 15 of the probe 104 from the tip of the cannula 102 may be indicated. by the distance or reference marks arranged on the rod 132 of the probe 104.

Once the probe 104 is located within the fibrous ring "A" as desired, the power source 106 is activated, whereby the probe 104 releases thermal energy and / or creates an electromagnetic field adjacent to the intervertebral disc "D" to produce the desired thermal and / or EMF therapy. Appropriate amounts of power, current intensity, or heat can be monitored from power source 106 and released for a certain amount of time determined to be adequate for clinical needs. For example, if the objective is the denervation of the nerves surrounding the intervertebral disc "D", the tissue adjacent to the exposed end of the probe 104 is heated to a temperature from about 45 ° C to about 60 ° C. If the surgical objective is the healing of the fissures in the intervertebral disc "D", the temperature in the tissue rises to approximately 60 ° C-75 ° C. 25

As one skilled in the art can appreciate, the degree and / or amount of exposure of the distal portion of the probe 104 of the tip of the cannula 102 controls the volume of disc tissue heated by the probe 104. Sensors ( not shown) to provide information regarding tissue temperature adjacent to probe 104. Alternatively, the impedance medium (not shown), associated with, for example probe 104, can provide measurements of tissue impedance, providing this mode an indication of the degree of desiccation, elevation 30 of the power or carbonization, which can take place near the exposed distal part of the probe 104. This indicates the effectiveness of the treatment.

Turning now to Figures 7-16, according to the present disclosure, a method of performing a surgical procedure using thermally profiled electrode layers is illustrated and described. The method includes the step of providing a system 100 for using RF energy and the thermal profile in surgical procedures (Step 1). As described above, the system 100 preferably includes an introducer cannula 102, at least one probe 104 that can be placed inside the cannula 102, a set of images 200 that includes a plurality of layers 202, and a formation system of 300 images configured and adapted to take images of an objective surgical site and visualize the images of the objective surgical site to the operator.

The method of performing the surgical procedure includes the steps of: 40

 imaging the target surgical site with the imaging system 300 in order to visualize the target surgical site on the monitor 304, see Figures 7 and 10;

 selecting a layer 202 of a plurality of layers 202 stored in the set of images 200 in relation to the desired treatment effect of a specially shaped probe;

 superimpose the selected layer 202 on the target surgical site, see Figures 7, 11, 12, 14 45 and 15;

 evaluate the scope, degree and / or depth of the treatment provided to the target surgical site using and / or configuring system 100 with the parameters corresponding to and / or associated with the selected layer 202;

 insert a cannula / probe assembly 102/104, which includes a probe 104 corresponding to the 50 electrode parameters of the selected layer 202, at the target surgical site, see Figures 11 and 15; Y

 activate and / or stimulate probe 104 according to the parameters corresponding to and / or associated with the selected layer 202.

In an alternative method, probe 104 is inserted into the target surgical site (see Figures 11 and 13) before superimposing layer 202 on it. With the probe 104 in position the various layers 202 overlap on the probe 104 in order to illustrate the various possible thermal penetration depths and in order to determine the desired and / or appropriate operating parameters and / or probe activation 104, see Figures 12, 14 and 15. A layer 200 corresponding to a desired surgical effect is selected. The probe 104 is then activated according to the parameters of the selected layer 202.

In any of these methods the selected layer 202 provides the operator with a visual representation of the depths of thermal penetration produced by the probe 104 when it is graduated in the parameters of the selected layer 202. In addition, the selected layer 202 allows the operator to visualize better the desired placement of the probe 104 and / or allows the operator to guide the probe 104 to the target surgical site along a path that corresponds to the direction of the thermal profile of the selected layer 202. In addition, the thermal displays offered by the Layers 202 can help identify mechanisms of action and optimize desired effects. In addition, the operator can compare the various effects of a variety of electrodes in different ways to optimize the surgical outcome.

Figures 13-16 are fluoroscopic images of the spine that illustrate the steps of the methods described above.

The application and use of layers 202 on monitors 304 can range from simple systems in which the operator manually places layer 202 on monitor 304 to sophisticated pattern recognition systems. Pattern recognition systems could be used to identify the treatment parameters selected by the operator, select the appropriate layer 202 from the set of images 200, and project and / or 20 visualize the layer 202, at an appropriate scale and placement, in the monitor 304. As can be seen, this allows the surgeon to visualize and estimate the result of the treatment and the general effect on the tissue (for example thermal propagation) before energizing the electrode.

While the above description contains many specific examples, these should not be interpreted as limitations on the scope of the exposure, but only as an exemplification of preferred embodiments thereof. Those skilled in the art will consider that there may be other possible variations that fall within the scope of the invention defined by the claims appended thereto.

Claims (10)

1. A system for the thermal or electromagnetic treatment of an objective surgical site (D), the system comprising: a cannula (102) having a proximal and a distal end; a probe (104) for the release of energy having a proximal and a distal end, the probe being able to be selectively advanced within the cannula to expose the distal end of the probe from the distal end of the cannula; and characterized because: a set of images (200) that includes a plurality of layers (202n), each layer including an image representing a treatment profile for the probe, the treatment profile estimating a therapeutic treatment depth 10 by the activation of the probe, wherein the image of each layer represents a thermal profile (150) surrounding the exposed distal end of the probe. 2. The system according to claim 1, wherein each layer is a digital representation. 3. The system according to claim 1 or 2, wherein the distal end of the probe can be exposed from the distal end of the cannula to approximately 6 mm. 4. The system according to claim 1, 2 or 3, which further includes an imaging system (300) showing the target surgical site on a screen (304). 5. The system according to claim 4, wherein the imaging system is an operative association with the set of images that are superimposable on the image of the target surgical site. twenty 6. The system according to claim 1, wherein the probe is adapted to be connected to a power source (100). 7. The system according to claim 6, wherein the power source can be adjusted to vary at least a selected operating graduation of at least one of temperature, impedance, RF power, RF current intensity, RF voltage, mode of operation and duration of application. 25 8. The system according to any of the preceding claims, which further comprises at least one layer for each amount of exposure of the distal end of the probe from the distal end of the cannula. 9. The system according to claim 8, wherein at least one layer for each amount of exposure of the distal end of the probe includes at least one layer for each operational graduation of the power source. 10. The system according to claim 1, wherein each layer represents a treatment profile that corresponds to one of a plurality of probe configurations and unique intensity graduations.